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rs1801002(G;T)

From SNPedia
Carrier of a recessive deafness mutation
Is agenotype
ofrs1801002
GeneGJB2
Chromosome13
Position20,189,547
mentionedby
Magnitude3
ReputeBad
Geno Mag Summary
(G;G) 0 common in clinvar
(G;T) 3 Carrier of a recessive deafness mutation
(GT;GT) 0 common in clinvar
(I;I) 0

see GJB2 and deafness